EndaCof DM Brompheniramine Maleate, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride 1 mg/5mL; 5 mg/5mL; 2.5 mg/5mL Liquid, 473 mL — NDC 68047-143-16 (Billing 68047-0143-16)
This is a package of 473 mL of EndaCof DM Brompheniramine Maleate, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride 1 mg/5mL; 5 mg/5mL; 2.5 mg/5mL Liquid from Larken Laboratories, Inc., marketed since Mar 2012 and currently FDA-listed; retail pharmacies pay about $0.0512 per mL (NADAC). It is this product's only package size.
NDC database record
One package, one record: these facts belong to NDC 68047-143-16 alone.
- Record
- FDA NDC Directory package listing · Human OTC drug
- Code segments
- 68047 labeler · 143 product · 16 package
- Package marketed since
- Mar 30, 2012
- Sample package
- No — commercial package
- Listing certified through
- Dec 31, 2026
- Billing quantity
- 473 mL per package
- Barcode (UPC)
- 0368047143167
- Medicaid fills, this package
- 18,287 prescriptions in the last four reported quarters
- FDA record last changed
- Jul 24, 2026
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
Drug-database identifiers Medi-Span GPI and First Databank GCN / HICL / AHFS classification
- GSN (GCN sequence number): 060622
- GCN: 26808
- GPI-14 (Medi-Span): 43995803080910
- HICL (First Databank): 035368
- AHFS class code: 04:04.20.00
- RxCUI (RxNorm): 1090463
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 5, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 1, 2026
RxNorm drug class
This medicine belongs to the Substituted alkylamines class.
Where does this data come from?
- RxClass (NLM) · catalog refreshed Oct 1, 2026
Clinical
Brompheniramine is used to treat allergy and cold symptoms: sneezing runny nose itching of the nose or throat red, itchy, watery eyes Brompheniramine is in a class of medications called antihistamines. It works by blocking the action of histamine, a substance in the body that causes allergic symptoms.
Read the full MedlinePlus article ↗EndaCof DM is an over-the-counter oral liquid cough and cold product containing three active ingredients. Brompheniramine maleate is an antihistamine typically used to reduce allergy-related symptoms and congestion. Dextromethorphan hydrobromide is a cough suppressant commonly found in cold remedies. Phenylephrine hydrochloride is a decongestant typically used to relieve nasal congestion. This product is marketed under FDA's over-the-counter drug monograph rules.
Patient education
Supplement & herbal interactions
Where does this data come from?
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 5, 2026
Ask a licensed pharmacist directly — free, answered by our team.
Pricing
A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.
| Price system | Per mL | Per package |
|---|---|---|
| Retail pharmacies payNADAC · weekly | $0.051 | $24.22 / 473 ml |
| Medicaid paysCMS SDUD · 12 mo | $0.0885 | $41.86 / 473 ml |
| Medicare drug plans payPart D · quarterly | No Part D plan price is available for this NDC in our data. | |
Where does this data come from?
- CMS NADAC weekly file · file of Sep 30, 2026
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · through Q1 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 68047-0143-16 You're viewing this Main listing | 473 mL in 1 BOTTLE | 2012-03-30 | — | Active |
Therapeutic equivalents
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA Orange Book · refreshed Oct 3, 2026
- CMS NADAC weekly file · file of Sep 30, 2026
Availability & generic status
We did not find an FDA-approved generic match for this exact strength, form and route.
Where does this data come from?
- FDA Orange Book · refreshed Oct 3, 2026
Inactive Ingredients / Excipients
Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.
💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.
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UNII 8SKN0B0MIM
Benzoic acid is a naturally occurring organic acid used as a preservative in medicines and foods. It helps prevent bacterial and fungal growth to extend shelf life and maintain product stability.
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UNII 7FLD91C86K
Edetate disodium is a chemical compound that binds and removes certain metal ions. In medicines, it acts as a preservative and stabilizer by preventing metals like calcium from interfering with the product's shelf life and consistency.
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UNII WZB9127XOA
A synthetic red dye used to color medications and make them easier to identify. It serves as a colorant in tablets, capsules, and liquid formulations.
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UNII 6DC9Q167V3
Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
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UNII SB8ZUX40TY
Saccharin sodium is an artificial sweetener made from saccharin salt. It's added to medicines to improve taste, especially in liquid formulations for children or bitter drugs.
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UNII 506T60A25R
Sorbitol is a natural sugar alcohol derived from glucose. It serves as a sweetener, humectant, and bulking agent in medications to improve taste and help maintain moisture in the product.
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UNII 059QF0KO0R
Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.
7 inactive ingredients listed in the exact product block matched to this NDC.
Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.
Where does this data come from?
ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.- FDA label on DailyMed · label index refreshed Oct 5, 2026
- FDA openFDA NDC Directory · synced Oct 1, 2026
Inactive ingredient FAQ
Are inactive ingredients the same for every manufacturer?
Why might an inactive ingredient be missing?
Can inactive ingredients matter?
Manufacturer & labeler
More NDCs from Larken Laboratories, Inc. labeler code 68047
- LoHist D Chlorpheniramine Maleate / Pseudoephedrine HCl 2 mg/5mL; 30 mg/5mL Liquid NDC 68047-120-16
- LoHist DM Brompheniramine Maleate, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride 10 mg/5mL; 5 mg/5mL; 2 mg/5mL Liquid NDC 68047-129-16
- LoHist-D Chlorpheniramine Maleate / Pseudoephedrine HCl 2 mg/5mL; 30 mg/5mL Liquid NDC 68047-159-16
- NoHist DM Chlorpheniramine Maleate, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride 4 mg/5mL; 10 mg/5mL; 15 mg/5mL Liquid NDC 68047-186-16
- OSCIMIN Hyoscyamine Sulfate .125 mg Tablet NDC 68047-252-01
- OSCIMIN Hyoscyamine Sulfate .125 mg Tablet, Orally Disintegrating NDC 68047-253-01
- Dexamethasone 1.5 mg 1.5 mg Tablet NDC 68047-702-01
- Doxycycline Hyclate 20 mg Tablet NDC 68047-714-01
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 2026
- Drugs@FDA
FDA label — Drug Facts FDA SPL
🎯 Indications and Usage ▾
Uses Temporarily relieves these symptoms due to hay fever (allergic rhinitis): cough due to minor throat and bronchial irritation runny nose sneezing itchy, watery eyes itching of the nose or throat temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies temporarily restores freer breathing through the nose
⏱️ Dosage and Administration ▾
Directions Do not exceed 6 doses in a 24-hour period Age Dose Adults and children over 12 years of age: 4 teaspoonsful (20 mL) every 4 hours Children 6 to under 12 years of age: 2 teaspoonsful (10 mL) every 4 hours Children under 6 years of age: Ask your doctor
⚠️ Warnings ▾
Warnings Do not use to sedate a child or make a child sleepy if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this drug.
🧪 Active Ingredient ▾
Active Ingredients (In each 5 mL teaspoonful) Brompheniramine Maleate, USP 1 mg Dextromethorphan HBr, USP 5 mg Phenylephrine HCl, USP 2.5 mg
🧪 Inactive Ingredients ▾
Inactive Ingredients Benzoic acid, edetate disodium, FD&C Red #40, propylene glycol, purified water saccharin sodium, sorbitol solution and strawberry flavoring
🎯 Purpose ▾
Purpose Brompheniramine Maleate Antihistamine Dextromethorphan HBr Antitussive (cough suppressant) Phenylephrine HCl Nasal decongestant
📄 Ask a Doctor Before Use If ▾
Ask a doctor before use if you have heart disease high blood pressure thyroid disease diabetes glaucoma trouble urinating due to an enlarged prostate gland a breathing problem such as emphysema or chronic bronchitis a cough that lasts or is chronic such as occurs with smoking, asthma or emphysema a cough that occurs with too much phlegm (mucus)
📄 Ask a Doctor or Pharmacist Before Use If ▾
Ask a doctor or pharmacist before use if you are taking any other nasal decongestant or stimulant taking sedatives or tranquilizers
📄 When Using This Product ▾
When using this product Do not exceed recommended dosage. marked drowsiness may occur avoid alcoholic beverages alcohol, sedatives, and tranquilizers may increase drowsiness be careful when driving a motor vehicle or operating machinery excitability may occur, especially in children
📄 Stop Use and Ask a Doctor If ▾
Stop use and ask a doctor if nervousness, dizziness, or sleeplessness occur. cough or nasal congestion persists for more than 1 week, tends to recur, or is accompanied by a fever, rash or persistent headache. These could be signs of a serious condition.
🤰 If Pregnant or Breast-Feeding ▾
If pregnant or breast-feeding ask a health professional before use.
📄 Keep Out of Reach of Children ▾
Keep out of the reach of children In case of overdose, get medical help or contact a Poison Control Center immediately.
📄 Questions or Comments ▾
Questions or Comments Call 1-601-855-7678 weekdays from 9:00 am to 4:00 pm CST or go to http://www.larkenlabs.com .
📄 Package Label / Principal Display Panel ▾
Principal Display Panel Figure 1: 16 oz. Bottle Label (Front) figure-01
Principal Display Panel Figure 2: 16 oz. Bottle Label (Drug Facts Continued) figure-02